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A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Fire needle therapy is an effective and better alternative to surgery for early-stage neck carbuncles.

Pegvaliase effectively reduces blood phenylalanine levels in most PKU patients, but requires personalized plans and good communication to manage side effects.

The patient recovered well and returned to college without any lasting issues.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Treatment with methotrexate and prednisolone led to complete hair regrowth and no relapse for 2 years.

Improving oral hygiene and quitting smoking can resolve black hairy tongue.

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

A cat with ear infection and skin issues was successfully treated for Demodex mites using imidacloprid and moxidectin.

The case suggests a possible link between severe acne and certain bone deformities.

A COVID-19 patient had severe and long-lasting skin issues and unusual hair loss.

Thermography matched the patient's pain levels in a shingles case and might help diagnose shingles without a rash.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

Hair loss linked to prostate enlargement; stress and family history important factors.

Early diagnosis, intensive therapy, and careful follow-up are crucial for managing overlapping TTP and SLE.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A woman's heart failure improved after she added vitamins and changed her diet from only cheese chips and cake.

A patient with a rare form of lupus improved after treatment for skin ulcers and hair loss on the face and scalp.

Taking Propecia might lead to the development of cataracts.

A man developed a rare late-onset hair-pulling disorder, usually seen in younger people.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The fractional ultrapulse CO2 laser is a safe and effective non-surgical treatment for upper eyelid issues and brow lifting.

Gore-Tex is effective for severe congenital ptosis, with the open approach better for no lid crease and the closed approach better for a preserved crease.

Acne is strongly linked to high BMI, hair loss, menstrual issues, family history, and eating too many sweets and fatty foods, but not to excessive hair growth.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.